Azo compounds and material colored therewith



Patented May .6, 1941 AZO COIVIPOUND'S AND TH EREW'ITHv comes Joseph B. Dickey, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey No Drawing. Application April 30, 1940,

V Serial No. 332,581

17 Claims. (01. etc-26c) This invention relates to the art of dyeing or coloring. More particularly it relates to new aromatic azo dye compounds and the application of the nuclear non-sulfonated compounds for the coloration of organic derivatives of cellulose especially textile materials made of or containing an organic derivative of cellulose by dyeing printing, stenciling or like methods.

Organic derivatives of cellulose are characterized by an indifierent affinity for the usual cotton and wool dyes'especially the ordinary water soluble dyes. Because of this, it has been necessary to develop new dye compounds suitable for the dyeing or coloration of materials, such as textile materials, made of or containing an organic derivati'veof cellulose. It is, accordinglyan object of my invention to provide a new class of azo dyes suitable for the'dyeing or coloration of organic derivatives of cellulose. Another object is to provide a process for the coloration of organic derivatives of cellulose in which the dye or dyes are applied directly from an aqueous suspension to the materials undergoing coloration. A further object is to produce dyeings on'organic derivatives of cellulose which are of good fastness to light and washing. Other objects will hereinafter appear.

Typical organic derivatives of cellulose include the hydrolyzed as wellas the unhydrolyzed cellulose organic acid esters such as celluloseacetate,

cellulose formate, cellulose propionate, or cellulose butyrate and the hydrolyzed as well as the unhydrolyzed mixed organic acid esters of'cellulose such as cellulose acetate-propionate, cellulose acetate-butyrate, and the cellulose ethers such as methyl cellulose, ethyl cellulose, or benzyl cellulose. While my invention will be illustrated more particularly in connection with the coloration of cellulose acetate, a material to which the invention is especially adapted, it will'be'understood that it applies to the coloration of other organic derivatives of cellulose such as those just mentioned. g

The azo dye compounds of my invention have the general formula:

RN=N-R1 wherein R represents theresidue of an aromatic nucleus and R1 represents the residue'of a henzene nucleus having but one benzene ring containing a Ra N.

1 and an acid ester of an acid of phosphorus group,

group, wherein R2 and R3 each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown. Advantageously R is the residue of an aryl nucleus of the benzene series containing but one benzene ring. I

While my invention relates broadly to the azo dye compounds having the above formula, it relates more particularly to the azo dye compounds having the general formula:

wherein R, R2 and R3 have the meaning previously assigned to them and R4 represents a member selected from the group consisting of 0 0 V o 0 o o and an'acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-formingv metal.

lustrative of furyl may be mentioned furfuryl, tetrahydrofurfuryl, -ethyltetrahydrofurfuryl and 5-shydroxyethyltetrahydrofunfuryl. Again, it will be understood that the expression a phenyl group includes not only phenyl but phenyl groups substituted, for example, with a halogen atom such as chlorine and. bromine, an alkyl group, a hydroxy group and a nitro group.

The azo dye compounds of my invention can be prepared by diazotizing suitable primary aromatic amines and coupling the-diazonium. com-- pounds obtained with benzene coupling com-....

pounds containing a group, wherein R2 and R3 have the meaning previously assigned to them, and a member selected l group nogroup should. be present in the benzene nucleus which would prevent coupling in this position. 7

Suitable aromatic amines that can beemployed in the preparation of the azo dye compounds of my invention include, for example, p-nitroaniline, 1-amino-2,4-dinitro-fi-chlorobenzene, 1- amino 2 nitro 4 chlorobenzene, 1-amino-2- bromo-4-m'trobenzene, l-amino-ZA-dinitrobenzene, l-amino-ZA-diChld-iO-(or bromo) benzene, p-aminoacetophenone, l-amino 2,4 dinitro-6- cyanobenzene, .1-aminoe2-chloro 4-methylbenzene, '1-amino-2-methyle4-.bromobenzene, 1- amino 2-- propylrl-chlorobenzene, p-aminoazobenzene, naphthylamine, 1-amino-5-naphthol, 1-amino-4-nitronaphthalene, 'p-aminobenzophenone, p-aminobenzenesulfonamide,' methyl anthranilate, l-aminoe i-ethylamino anthraquinone, l-amino- 4- phenylamino, anthraquinone, 2- aminobenzothiazole and Z-amino-G-methyl benzothiazole. 5 1 1 Suitable coupling components that can the employed in the preparation of the compounds of my invention include, for example, o-acetyl di-phydroxyethylaminophenol, m-propionyl mono-pmethoxyethylaminophenol;

3-( 04c ')-mono--y-hydroxypropylaniline 5 -mono-iurfurylaniline -6-methyl-mono butylaniline o-o H2-O CzHsymono-allylaniline o and 3- -.0S0tetrahydromrmry1 '-6-methoxy-monog crotonylanlline It will be understood that in the nomenclature employed above the amino group occupies the 1 position.

,Ihe azo dye compounds of my invention, depending upon their structure,constitute valuable dyes for the coloration of organic derivatives'of cellulose,'wool.and silk. As previously indicated the nuclear non-sulfonated azo dye compounds can be employed for the coloration of organic derivatives of cellulose such as those hereinbefore mentioned yielding variousIshades thereon of good fastness to light and washing. These nuclearnon-sulfonated dye compounds likewise possess some application for the coloration'of wool and'silk and yield generally similar shades on these materials as on organic derivatives of cellulose. ,The.nuclearsulfonated compounds of my invention possess-little or no-utility for the Ewamplel 12.8 grams of o-chloroaniline are dissolved in 200 grams of a Water and ice mixture to which has zbeen added 25 cc. of 36% hydrochloric acid. The resulting solution. is cooled ifnecessary to about 05 C. and the o-chloroaniline is ,diazotized by adding with stirring 6.9 grams of sodium nitrite dissolved in water while maintaining the temperature at about 0-5 C.

18.9 grams of m-acetyl dimethylaminophenol are dissolved in glacial acetic acid and the resuiting solution is cooled to a temperature approximating -10 CL The diazon'ium solution prepared as described above is then slowly added with stirring while maintaining a temperature of (1-10" C. following which the mixture is immediately made neutral to Congo red paper by the addition of sodium acetate. Upon completion of the coupling reaction the dye compound formed" azonium compound obtained .is coupled with .1 grammole of o( i-cH2-ocna r. 1.. I i

ill...

Coupling and recovery of the dye compound formed can be carried out in accordance with the general procedure described in Example 1. The dye compound obtained colors cellulose acetate silk violet.

Equal molecular weights of 1-'amino-2,4,6-trinitrobenzene; 2,4-dinitro-a-naphthylamine and 1- pound obtained colors cellulose acetate silk orange.

Example 3 13.8 grams of p-nitroaniline are diazotized in known fashion and the diazonium compound obtained is coupled with 24.3 grams of 3-acetyl-6- methoxy ethyl-p-hydroxyethylaminophenol,

Coupling and recovery of the dye compound formed can be carried out in accordance with the method described in Example 1. The dye compound obtained colors cellulose acetate silk red.

An equivalent gram molecular weight of cyclohexanol can besubstituted for the coupling component of this example to obtain a dye compound colors cellulose acetate silk red.

Example 4 I group.

which 21.7 grams of l-amino-2-bromo-4-nitrobenzene L are diazotized in known fashion and the diazonium compound obtained is coupled with .1 gram mole of 0-c-cmomom O CH2CH2SOaNa C HaCHzCHaCHs CH2 Coupling and recovery of the dye compound formed can be carried out in accordance with the general procedure described in Example 1. The dye compound obtained colors cellulose acetate silk ru'bine.

Example 5 26.2 grams .0: 1-amino-2,4-dinitro-6-bromoanl line are diaz otized in known fashion and the diamino-4-mehylaminoanthraquinone can be substituted for the diazo component of the example to obtain dye compounds of my invention.

Example 6 .1 gram molecular weight of is dissolved in dioxane and treated with .1 gram molecular weight of sodium carbonate and an equivalent amount of p-toluenesulfonyl chloride. By this'reaotion a dye Product of my invention is obtained in which the hydroxyl group shown in the above formula is converted to a In" place of p-toluene sulfonyl chloride,

OHsOHzOHnOH2OB-Cl I; can be employed to obtain dye compounds of my invention. Example 7 gram mole of 1-amino-2,4-dinitro-fi-chlorobenzene is diazotized in known fashion and the di-azonium compound obtained is coupled with .1 gram mole of Coupling and recovery of the dye compound formed can be carried out in accordance with the general method described in Example 1. The dye compound obtained colors cellulose acetate silk greenish-blue.

.Igram mole of l-amino-2,4-dinitrobenzene can be substituted for the diazo component of the above example to obtain a. dye which similarly colors cellulose acetate silk a greenish-blue shade. 8

.1 gram mole of 2-amino-5-nitrophenylmethyl- ,sulf one are diazotized in known fashion and the diazonium compound obtained is coupled with .1

I grammole of 3-methyl-fi-acetoxy-di-p-hydroxy- 'ethylaniline. Coupling and recovery of the dye compound formed can be carried out in accord- 0 00m cmomcmo-soma group instead of the ester group present in the compounds of the present invention.

The following tabulation further illustrates the compounds included withinvthe scope of my invention together with the colors they produce on cellulose acetate silk. The compounds indicated below may be prepared by diazotizing the amines listed under the heading Amine and coupling the diazonium compounds obtained with the compounds specified in the column entitled Coupling- /R| component. The diazotiz'ation and coupling reactions may, for example, be carried out follow-V R: ing the general procedure described in Examples 1 to 8, inclusive.

Amine Coupling component Color o -(F,Cl,Br,I)-aniline (1) CH: Yellow.

.7 l. r l 1' a -C-C Hs \CBHB Do (2) 0112011103 Do.

I \CHBCHIOH O-COC2H5 2', "D0 (3) V CHzCHaCH: Do.

D0 (4) CHzCHOHCH: Do.

S-OH H V 0 o Du 5 CH5 CHzCHaCHaCHs D0. O t \H OCH: A-CHzCHn-O-P ONa Do (6) H2C-CH:V Do. CH: /H

N/ \O/ CHs OS0H 1 t 'VDO u (7) cyclohexyl D0- H o-o-on CHQCH=CH1 l l lS!O- -cyclohery1 Amine boupling component Color -(F,Cl, Bl,I)-8l1i1il18 (9) ONa Yellow.

- omom-o-r CHIC O O Na .|l-CH2CH5 Dn 11 o-omomsoma p /cyclohexanol (o, m or p) C H (].|2CH:

l-amino-2,4-diehlorobenzene 1 to 11 inclusive. Orange-yellow. l-emino2-chloro-4-bromob mm Do. 1-amino-2,5-dibromobenzene Do. 1-an1ino-2-chloro-fi-bromobenzene. Do. o-mtroaniline. Orange-red. m-nitroaniline Orange. p-nitroaniline Red. l-amino-Z-nitro-kchlorobenzene. 1-amino-2-chloro-4-nitrobenzenel l-amino-Z-methoxyi-nitrobenzen 1-amino-2-phenoxy-4-nitrobenzene. p-aminoacetophenone p-aminobenzophenone D i Lamina-2, 4-dinitro-6-ch1orobenzene;; Purple. 2,4-dinitr0-a-naphthylamino Bluish-purple. Z-amino-fi-nitrophenyl methyl sulfone Rubme. Z-amino-E-nitromethyl benzoate Do. 2-amino-3,fi-dinitrobenzamide. Purple. 1-amino-2-phenoxy-4-chlor e Orange-yellpw.

In order to avoid possible confusion it is here noted that the coupling components designated o-acetyl di-p-hydroxyethylaminophenol and mpropionyl mono-,8-methoxyethylaminophenol refor to Sulfonated amines which can be diazotized and the diazonium compounds obtained coupled with any of the coupling components shownherein to obtain dye compounds of my invention include, for example, p-sulfanilic acid, l-amino-i-sulfonic naphthalene, 2-naphthylamine-8-sulfonic acid, 1-naphthylamine-3-sulfonic acid, l-naphthylamine-E-sulfoni-c acid, l-naphthylamine-S- sulfonic acid, 1 naphthylamine 4,8 disuli'onic acid, 1-naphthylamine-3,8-disulfonic acid, -1-

amino--naphtho1-7 -sulfonic acid, metanlilic acid,

1-amino-2-sulfonic-4-nitrobenzene, 1-ami'rio -2, 4

dis ulionic benzene and l-amino-Z-chloro-Lsulfonic benzene.

In order that my invention may be completely understood, the preparationof various coupling components employed in the preparation of the compounds of my inventionis described hereinafter.

The coupling components of my invention can ordinarily be prepared from compounds having the general formula:

z -o-o1 the I 'O-C- Z grouping canlbe introduced in ortho or meta vposition to'tl ie- .I o r with one gram mole of ethylene oxide at 180 C.

group. Similarly by reaction with compounds having the general formula Ol-O-S-Z the -o-s z grouping can 'be introduced in ortho or meta po 1 O sition to the group. This latter reaction is shown in Example 6. Z in the formulas just given is aliphatic, phenyl or furyl.

Further by reaction with compounds having the general formula grouping can be introduced by reacting the compounds above mentioned having the general formula:

' /R: N ,5 I ia 5 with chlorocarbonate compounds such as the furyl-, alkyland phenyl -chlorocarbonates. Compounds having the -Ofi-OY 5O grouping can be prepared by reacting the above mentioned compounds with sulfonyl chlorides such as methyl sulfonyl chloride, ethyl sulfonyl chloride and phenyl' sulfonyl chloride, for example.

The following examples illustrate the preparation of the coupling components of my invention.

Example A One gram mole of 2-methoxy-5-hydroxy-1- ethylamino benzene is heated in an autoclave for 6 hours. The reaction product resulting is cooled, removed from the reaction vessel and distilled under reduced pressure. The Z-methoxy- 5-hydroxy-1-(ethyl, hy'droxyethyD-amino benzene obtained is dissolved in dilute sodium hydroxide and treated with an equivalent amount of acetyl chloride. 2-me'thoxy-5-acetoxy-l-(ethyl, hydroxyethyl)-aminobenzene is formed and can be recovered by distillation under reduced .7 pressure.

Example B One gram mole of 1-nitro-3,5 dihydroxybenzene is reacted with one gram mole of methoxy acetic anhydride at 50 "C. to form 1-nitro-3-hydroxy-5-methoxy acetobenzene, which is in turn treated in cold dilute alkali with an equivalent gram molecular weight of tetrahydrofuro-yl chloride. The resulting diester is purified by crystallization from alcohol and reduced to the amino compound in alcohol with hydrogen and nickel. The amino compound formed is treated in benzene with sodium bicarbonate and allyl bromide to give the coupling component employed in Example 5.

From the foregoing it is believed that the preparation of the coupling components employed in the preparation of the azo dye compounds of my invention will be clearly understood by those skilled in the art to which this invention relates;

In addition we would here note that coupling compounds of the general formula wherein R2 andRa have the meaning previously assigned to them and R4 represents an acid ester of an acid of phosphorus group attached to the benzene nucleus in ortho or meta position to the group can be prepared by reacting compounds having the general formula I wherein R2 and R3 have the meaning previously assigned to them and wherein the hydroxy group is attached to the benzene nucleus in ortho or met-a position to the group with a phosphating agent. Phosphating agents which can be employed to prepare phosphoric and thiophosphoric acid esters are described in U. S. Patent No. 2,183,998, issued December 19, 1939. Phosphating agents which can be employed to prepare phosphorous acid esters include phosphorus trichloride and those described in application Serial No. 266,646, filed April '7; 1939.

The azo dye compounds of my invention are, for the'most part, relatively insoluble in water. Those compounds whichare insoluble in water may be advantageously employed for the direct dyeing of textile materials by grinding the dye to' a fine powder, intimately mixing it with'a suitable dispersing or solubilizing agent and adding the resulting mixture to water or a dilute solution of soap in water toform an aqueous dyebath. Following this known preparation of the dyebath, the textile material to be dyed may be added to the dyebath and the dyeing operation conducted in known fashion. The dye compounds of my inventionwhich are water soluble do not, of course, require the formula:

use of a; dispersing or solubilizing agent but may be applied to silk, wool and (dependingupon the nature and position of the water solubilizing group) organic derivatives of cellulose textile materials from an aqueous solution of the dye which may contain salt. For a more complete description as to how the azo dye compounds of my invention may be employed in dyeing or coloring operations, reference may be had to McNally and Dickey U. S. Letters Patent No. 2,115,030, issued April 26, 1938. For amore detailed description 'as to how the water soluble azo dyes of my invention may be employed for the coloration of textile materials made of or containing organic derivatives of cellulose, silk and wool or mixtures of these, reference may be had to McNally and Dickey U. S. Patent No. 2,107,898, issued February 8, 1938.

I claim:

1. The azo dye compounds having the general R--N=NRi wherein R represents the residue of an aromatic nucleus and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and R3 each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of 1 and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

2. The azo dye compounds having the general formula:

RN=NR1 wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and Ra each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of CZ,-O-0OY,Ofi-OY,-O;S Z,-O-S--0Y I! ll O 0 and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

'3. The azo dye compounds having the general wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and R3 each represents an aliphatic group and R: may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

4. The azo dye compounds having the general formula wherein R represents the residue of an aromatic nucleus, R2 and R3 each represents a member selected from the group consisting of an aliphatic-, a cycloalkyl-, a phenyland a furylgroup and wherein R3 may be in addition hydrogen and R4 represents a member selected from the group consisting of and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal.

5. The azo dye compounds having the general formula:

silk colored with an azo dye compound and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and afuryl group and wherein Y may be in addition an alkali-forming metal.

6. The azo dye compounds having the general and an acid'ester of phosphorus group, wherein Y and'Z eachrepresents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl'group, apheny'l group and a -furyl group and wherein Y may be inaddition an alkali-forming metal.

7. The azo dye having the formula:

CzHsbH I V 8; The azo dye having the formula:

0 H H NC-CH3 OrHs I NO NN N i 'omorionornorr No,

s CH3 9. The azo dye having theforrnula:

' OOOH3 G1 I ll ,7 O /C2H4OH N02 blIH 1 CH3 7 10. Material selected from the group consisting of an organic derivative of cellulose, wool and having the general formula: 1 r

wherein R represents the residue of an aromatic nucleus and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and 'Rs each represents a member selected from the group consisting of c an aliphatic group, acycloalkylgroup; a phenyl group -;and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo, bond shown and a member selected from the group consisting of II H ll v I t Y o o o 0 and an acid ester of an acid of I phosphorus group, wherein Y and Z each represents a mem- RN=N--R1 wherein R represents the residue of an aromatic nucleus and R1 represents the residue of a benzene nucleushaving but one benzene ring containing a group, wherein R2 and Rs each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position tothe azo bondshown and a member selected from the group consisting of and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y maybe in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

12. An organic derivative of cellulose colored with a nuclear non-sulfonated azo dye compound having the general formula:

RN'=NR wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and R3 each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring, R2 and R3 each represents a member selected from the group consisting of an a1iphatic-, a cycloalkyl-, a phenyland a furylgroup and wherein R3 may be in addition hydrogen and R4 represents a member selected from the group consisting of o-o-z II o O-COY II -OIS'-OY o -o;sz o -o-s-oY and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a fury] group and wherein Y may be in addition an alkali-forming metal.

14. A cellulose acetate colored with a nuclear non-sulfonated azo dye compound having the general formula:

R,N=NR1 wherein R represents the residue of an aromatic nucleus and R1 represents the residue of a benzene nucleus having but one benzene ring containing a a group, wherein R2 and R3 each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of o O-fiJ-OY O-SIOY and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

15. A cellulose acetate colored with a nuclear non-sulfonated azo dye compound having the general formula:

wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and R3 each represents a member selected from the group consisting of an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

16. A cellulose acetate colored with a nuclear non-sulfonated azo dye compound having the general formula:

wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring and R1 represents the residue of a benzene nucleus having but one benzene ring containing a group, wherein R2 and R3 each represents an aliphatic group and R3 may be in addition hydrogen, attached thereto in para position to the azo bond shown and a member selected from the group consisting of and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hyrogen, an aliphatic group, a cycloalkyl group, a phenyl group and a furyl group and wherein Y may be in addition an alkali-forming metal, attached thereto in ortho or meta position to the azo bond shown.

17. A cellulose acetate colored with a nuclear non-sulfonated azo dye compound having the general formula:

wherein R represents the residue of an aryl nucleus of the benzene series containing but one benzene ring, R2 and R3 each represents a mem ber selected from the group consisting of an aliphatic-, a cy-cloa1ky1-, a phenyland a. furylgroup and wherein R3 may be in addition hydrogen and R4 represents a member selected from the group consisting of -O--fi-OY 0 -os-'z OSOY 0 o and an acid ester of an acid of phosphorus group, wherein Y and Z each represents a member selected from the group consisting of hydrogen, an aliphatic group, a cycloalkyl group, a

phenyl group and a furyl group and. wherein Y may be in addition an alkali-forming metal.

JOSEPH B. DICKEY. 

